Evidence map›Paper›PMID 38711644›Full record

ArticleHeliyon2024

Comparing GDF9 in mature follicles and clinical outcomes across different PCOS phenotype.

Jingjing Cai, Xiangmin Luo, Zhengyao Wang, Zixuan Chen, Donghong Huang, Hui Cao, Jing Chen, Jinxiang Wu

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In one paragraph

Article in Heliyon, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Jingjing CaiDepartment of Reproductive Medcine, the Second Affiliated Hospital of Fujian Medical University, Quanzhou, FuJian, 362000, PR China.
Xiangmin LuoDepartment of Reproductive Medcine, the Second Affiliated Hospital of Fujian Medical University, Quanzhou, FuJian, 362000, PR China.
Zhengyao WangDepartment of Reproductive Medcine, the Second Affiliated Hospital of Fujian Medical University, Quanzhou, FuJian, 362000, PR China.
Zixuan ChenDepartment of Clinical Laboratory, Fujian Medical University Affiliated First Quanzhou Hospital, Quanzhou, FuJian, 362000, PR China.
Donghong HuangDepartment of Clinical Laboratory, the Second Affiliated Hospital of Fujian Medical University, Quanzhou, FuJian, 362000, PR China.
Hui CaoDepartment of Reproductive Medcine, the Second Affiliated Hospital of Fujian Medical University, Quanzhou, FuJian, 362000, PR China.
Jing ChenDepartment of Reproductive Medcine, the Second Affiliated Hospital of Fujian Medical University, Quanzhou, FuJian, 362000, PR China.
Jinxiang WuDepartment of Reproductive Medcine, the Second Affiliated Hospital of Fujian Medical University, Quanzhou, FuJian, 362000, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Polycystic ovary syndrome (PCOS) is main cause of anovulatory infertility in women with gestational age. There are currently four distinct phenotypes associated with individualized endocrinology and metabolism. Growth differentiation factor 9 (GDF9) is a candidate as potential biomarker for the assessment of oocyte competence. The effect on oocyte capacity has not been evaluated and analyzed in PCOS phenotypes. Objective: We aimed to screen the expression levels of GDF9 in mature follicles of women with controlled ovarian hyperstimulation (COS) with different PCOS phenotypes. To determine the correlation between the expression level of GDF9 and oocyte development ability. Methods: In Part 1, we conducted a retrospective study comparing the clinical outcomes and endocrine characteristics of patients with PCOS according to different subgroups (depending on the presence or absence of the main features of polycystic ovarian morphology (PCOM), hyperandrogenism (HA), and oligo-anovulation (OA)) and non-PCOS control group. We stratified PCOS as phenotype A (n = 29), phenotype B (n = 18) and phenotype D (n = 24). In Part 2, the expression of GDF9 in follicular fluid (FF) and cumulus cells (CCs) were detected by enzyme-linked immunosorbent assay (ELISA) and immunohistochemistry, respectively. Results: In Part 1, the baseline clinical, hormonal, and ultrasonographic characteristics of the study population were matched with the presence or absence of the cardinal features of each PCOS phenotypes showed a clear difference. Phenotypes A and D had statistically significant associations with blastocyst formation and clinical pregnancy compared with phenotypes B ( Conclusions: GDF9 expression varies with different PCOS phenotypes. Phenotype A had higher GDF9 levels and blastocyst formation ability.

Indexed as

Blastocyst formationGDF9Mature folliclesOocyte competencePCOSPCOS phenotypes

Identifiers

PMID38711644
PMCPMC11070807

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